人毛囊冷冻保存用于器官培养:玻璃化法优于慢速冷冻
Cryopreservation of human hair follicles for organ culture
研究比较慢速冷冻与玻璃化两种方案保存人毛囊用于器官培养,玻璃化(15% DMSO 与 15% EG,液氮快速降温)细胞死亡少于慢速冷冻(10% DMSO,1 °C/min 降温),毛干伸长约为新鲜毛囊的 75%。玻璃化还诱导毛囊从生长期向退行期转变,该转变在器官培养中可被米诺地尔部分抑制。
- Article
- Open access
- Published: 03 November 2026
- Sayuri Hamano1,
- Ting Sun2,
- Mioto Nishino2,
- Tatsuto Kageyama1,2,3,
- Ayaka Nanmo1,3,
- Jieun Seo1,2,3 &
- …
- Junji Fukuda1,2,3
Scientific Reports (2026) Cite this article
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Abstract
Extracted human hair follicles are critically useful specimens for various purposes, ranging from basic research, such as skin and hair follicle biology, to applications, including hair drug testing and cell sources for regenerative medicine. The ability to cryopreserve hair follicles enables their use in large quantities at any desired time. This study investigated the feasibility of human hair follicles after cryopreservation using two approaches: slow freezing and vitrification. Slow freezing resulted in severe cell death and loss of hair shaft elongation in subsequent organ culture. Vitrification resulted in less cell death than slow freezing and approximately 75% hair shaft elongation relative to fresh hair follicles. Interestingly, vitrification induced a transition of the hair cycle from the anagen to catagen phase, which is a typical undesirable change in patients with alopecia. This transition was partially suppressed by minoxidil treatment in organ culture. These results suggest that, under the conditions tested, the vitrification protocol (15% DMSO and 15% EG with rapid cooling in liquid nitrogen) preserves human hair follicles substantially better than the slow freezing protocol (10% DMSO with cooling at 1 °C/min), and vitrification may provide beneficial hair follicle samples for testing hair drugs to alleviate the transition to the catagen phase.
Acknowledgements
This work was partially supported by the Kanagawa Institute of Industrial Science and Technology (KISTEC). We thank Almo Plastic Clinic and Tokyo Hair Transplant Cosmetic Surgery for their cooperation in providing human scalp specimens and for their assistance with the isolation of scalp skin.
Funding
This research was funded by Hoyu Science Foundation Research Grant, and Grants-in-Aid for Scientific Research (Kakenhi) (grant numbers JP25K01599 and JP23K26464). These funders had no role in the analyses or interpretation of the findings.
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Authors and Affiliations
Institute of Advanced Sciences, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa, 240-8501, Japan
Sayuri Hamano, Tatsuto Kageyama, Ayaka Nanmo, Jieun Seo & Junji Fukuda
Faculty of Engineering, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa, 240-8501, Japan
Ting Sun, Mioto Nishino, Tatsuto Kageyama, Jieun Seo & Junji Fukuda
Kanagawa Institute of Industrial Science and Technology, 3-2-1 Sakado Takatsu-ku, Kawasaki, Kanagawa, 213-0012, Japan
Tatsuto Kageyama, Ayaka Nanmo, Jieun Seo & Junji Fukuda
Authors
- Sayuri Hamano
- Ting Sun
- Mioto Nishino
- Tatsuto Kageyama
- Ayaka Nanmo
- Jieun Seo
- Junji Fukuda
Corresponding author
Correspondence to Junji Fukuda.
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The authors declare no competing interests.
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Cite this article
Hamano, S., Sun, T., Nishino, M. et al. Cryopreservation of human hair follicles for organ culture. Sci Rep (2026). https://doi.org/10.1038/s41598-026-78938-9
Received: 16 August 2026
Accepted: 29 October 2026
Published: 03 November 2026
DOI: https://doi.org/10.1038/s41598-026-78938-9
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来源:Nature Biotechnology · nature.com